Plasma Isolation from Human Peripheral Blood

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UCAN-U 0017 Version November 01, 2011 Page 1 of 5 Written By Name Function Date Signature Mark Klein Lab manager Verification Name Function Date Signature Prof.dr. A.B.J. Prakken Co-Chair CMCI Changes from last version Date of version Paragraphs Date of version Paragraphs

UCAN-U 0017 Version November 01, 2011 Page 2 of 5 Content 1. Subject... 3 2. Application... 3 3. Definitions and Abbreviations... 3 4. Principle... 3 5. Safety precautions... 3 6. Equipment and Accessories tools... 3 6.1 Equipment... 3 6.2 Accessories... 3 7. Samples... 4 7.1 Sample Collection... 4 7.2 Sample Processing... 4 8. Procedure... 4 9. Processing of the Results... 4 Documentation of cells... 4 10. Documentation... 4 11. Accompanied Forms/ Attachments/ Document... 5 12. Remarks... 5

UCAN-U 0017 Version November 01, 2011 Page 3 of 5 1. Subject This Standard Operation Procedure (SOP) describes a method to isolate plasma from blood using centrifugation. 2. Application Isolation of plasma from peripheral blood using centrifugation. 3. Definitions and Abbreviations PBMC = peripheral blood mononuclear cells RT = room temperature v/v = volume/volume rpm = rotations per minute ml = milliliter EDTA = ethylenediaminetetraacetic acid 4. Principle Blood plasma is the liquid component of blood, in which the blood cells are suspended. It makes up about 60% of total blood volume. It is composed of mostly water (90% by volume), and contains dissolved proteins, glucose, clotting factors, mineral ions, hormones and carbon dioxide (plasma being the main medium for excretory product transportation). Plasma is the supernatant fluid obtained when anti-coagulated blood has been centrifuged. The blood is mixed with an appropriate amount of anticoagulant like heparin, oxalate or ethylenediaminetetraacetic acid (EDTA). This preparation should be mixed immediately and thoroughly to avoid clotting. Process samples as soon as possible. If storage is necessary prior to processing, store the blood at room temperature, shielded from light. DO NOT refrigerate the cells. 5. Safety precautions Treat all blood and synovial fluid samples as infectious material. Wear disposable gloves. 6. Equipment and Accessories tools 6.1 Equipment Centrifuge Hettich Rotanta 46 (UMC# 99-000-2142) Easypet pipet (Eppendorf, Germany, 4006173) Pipets 10-1000 µl (Gilson, The Hague, The Netherlands) 6.2 Accessories 1.8 ml sterile polypropylene Nunc crytubes (Nalge Nunc, Roskilde, Denmark, 375418 15 ml sterile polypropylene conical tubes (Falcon/ Becton Dickinson, Erembodegem, Belgium, 352096)

UCAN-U 0017 Version November 01, 2011 Page 4 of 5 7. Samples 10 ml sodium-heparin vacutainer blood collection tubes (Becton Dickinson, Erembodegem, Belgium, 366480) 5 ml sterile disposable pipet (Falcon/ Becton Dickinson, Erembodegem, Belgium, 357543) 10 ml sterile disposable pipet (Falcon/ Becton Dickinson, Erembodegem, Belgium, 357551) Disposable gloves (Kimberly Clark, Zaventem, Belgium) Easyload 200 µl (741035) and 1000 µl (741000) sterile pipettips (Greiner Bio-one, Germany) 7.1 Sample Collection Whole blood should be drawn in sodium heparin tubes with a venoject vacuum system. 7.2 Sample Processing All handlings of the sample should be done in a biohazard safety cabinet will wearing gloves Store the plasma at 80 C. Use the remains for layering on the ficoll. 8. Procedure 1. In a centrifuge capable of safely spinning blood tubes, spin the blood at roughly 1000 rpm for 10 minutes at room temperature. 2. Remove the tubes from the centrifuge, and in a clean and safe environment, open the tubes to access the plasma located at the top of the specimen. Note: if you intend to immortalize lymphoblastoid cultures or perform sterile work on the remaining cells, this step must be performed in a biosafety cabinet. 3. Using a sterile transfer pipet or a 1000 µl pipettor, carefully transfer 2x 1.5 ml of the plasma into appropriately labeled screw-cap cryovial tube. If 2x 1.5 ml is not possible, transfer as much as reasonably possible without disturbing or collecting any of the pelleted cells. 4. As soon as possible, place and store the collected plasma at -80 C. 5. Use the remaining material for one or more of the desired processes (ie DNA, RNA, PBL). 9. Processing of the Results Documentation of cells Log the plasma s in the excel file plasma storage 10. Documentation Fill in the patient form as accurate as possible. Document each sample in the Isolation Notebook as follows Patient Protocol code (consists of protocol code in combination with a serial number)

UCAN-U 0017 Version November 01, 2011 Page 5 of 5 Isolate by Plasma Person who isolated the samples amount of plasma per cryovial. 11. Accompanied Forms/ Attachments/ Document Instruction manual centrifuge Instruction manual safety cabinet Instruction manual freezer Instruction manual refrigerator 12. Remarks Do not close the Nunc cryovials to tight, as this will break the inner seal. Screw top firmly but stop when resistance is experienced. ***END***